Plant DNA Extraction Research Articles

Evaluation and application of an efficient plant DNA extraction protocol for laboratory and field testing.

Nucleic acids in plant tissue lysates can be captured quickly by a cellulose filter paper and prepared for amplification after a quick purification. In this study, a published filter paper strip method was modified by sticking the filter paper on a polyvinyl chloride resin (PVC) sheet. This modified method is named EZ-D, for EASY DNA extraction. Compared with the original cetyl trimethylammonium bromide (CTAB) method, DNA extracted by EZ-D is more efficient in polymerase chain reaction (PCR) amplification due to the more stable performance of the EZ-D stick. The EZ-D method is also faster, easier, and cheaper. PCR analyses showed that DNA extracted from several types of plant tissues by EZ-D was appropriate for specific identification of biological samples. A regular PCR reaction can detect the EZ-D-extracted DNA template at concentration as low as 0.1 ng/μL. Evaluation of the EZ-D showed that DNA extracts could be successfully amplified by PCR reaction for DNA fragments up to 3000 bp in length and up to 80% in GC content. EZ-D was successfully used for DNA extraction from a variety of plant species and plant tissues. Moreover, when EZ-D was combined with the loop-mediated isothermal amplification (LAMP) method, DNA identification of biological samples could be achieved without the need for specialized equipment. As an optimized DNA purification method, EZ-D shows great advantages in application and can be used widely in laboratories where equipment is limited and rapid results are required.

DNA testing of suspected cannabis samples with exceptional morphology using a simple detection kit

Cannabis is the most abused drug in the world and molecular biology techniques for the analysis of cannabis have attracted attention in recent years. We report a case of three persons conspiring to possess cannabis-like leaf pieces for profit. We present the results of DNA testing by a simple kit on suspected cannabis samples with exceptionally shaped leaves. DNA was obtained from the samples of cannabis leaves by a simple and rapid procedure using a cannabis DNA detection kit or commercially available purified plant DNA extraction kit. Undiluted or diluted DNA solution was used as templates for amplification of cannabis-specific sequences by triplex PCR. The presence or absence of PCR amplicon was visually observed by a DNA chromatography detection system to determine whether the sample was cannabis or not. When the DNA was extracted by the simple procedure and used without dilution, PCR failed to identify cannabis samples. However, when purified DNA was used, PCR amplification was successful in identifying all cannabis samples. Notably, in case of DNA extracted by the simple procedure, 10 to 50-fold dilution of the solution reduced PCR inhibition and PCR amplification was successful. Although the quality of the DNA used as PCR template needs to be considered, simple DNA testing with a kit is very effective for identifying suspected cannabis samples with exceptional morphology.

RPA-PCR couple: an approach to expedite plant diagnostics and overcome PCR inhibitors.

DNA extraction can be lengthy and sometimes ends up with amplification inhibitors. We present the potential of recombinase polymerase amplification (RPA) to replace plant DNA extraction. In our rapid 'RPA-PCR couple' concept, RPA is tuned to slower reaction kinetics to promote amplification of long targets. RPA primers amplify target and some flanking regions directly from simple plant macerates. Then PCR primers exponentially amplify the target directly from the RPA reaction. We present the coupling of RPA with conventional, TaqMan and SYBR Green PCR assays. We applied the concept to strawberry Phytophthora pathogens and the Phytophthora identification marker atp9-nad9. We found RPA-PCR couple specific, sensitive and reliable. The approach may also benefit other difficult samples such as food, feces and ancient samples.

Extraction of high-quality genomic DNA and identification of different DNA barcoding markers for chickpea (Cicer arietinum L.)

The genetic studies of individual plants, especially self-pollinated species like chickpea need to be evaluated at the DNA level with the help of molecular markers for identifying genetic variations among the plants. High-quality DNA extraction is a prerequisite for genetic studies. Extraction of intact genomic DNA with high – molecular mass is essential for the study of many molecular biology applications like Polymerase Chain Reaction, endonuclease restriction digestion, southern blot analysis, and also for the construction of a genomic library. Several plant DNA extraction methods are available, even though the DNA isolation methods that give good yield employing both quantity and quality is quite difficult especially for self-pollinated crops like a chickpea. This work was focused on developing a standard protocol for the extraction of genomic DNA and identifying different barcoding markers. The result revealed that the CTAB extraction method with slight modification in protocol had been optimized for DNA isolation. The purified DNA, which was isolated through the CTAB method, had excellent spectral qualities and is efficiently digested by a restriction endonuclease, and is found to be more suitable for long-fragment PCR amplification. DNA barcoding is considered as a promising tool because it provides a practical and standard identification of plants. The isolated DNA sample was processed with a classical DNA barcoding approach by amplifying and sequencing with a universal primer. According to the result, among the different barcoding markers studied, the RbcL and Mat K were found to given the best result for molecular species identification in chickpea.

DNA Extraction from Plant Leaves Using a Microneedle Patch.

Isolation of high-quality DNA from infected plant specimens is an essential step for the molecular detection of plant pathogens. However, DNA isolation from plant cells surrounded by rigid polysaccharide cell walls involves complicated steps and requires benchtop laboratory equipment. As a result, plant DNA extraction is currently confined to well-equipped laboratories and sample preparation has become one of the major hurdles for on-site molecular detection of plant pathogens. To overcome this hurdle, a simple DNA extraction method from plant leaf tissues has been developed. A microneedle (MN) patch made of polyvinyl alcohol (PVA) can isolate plant or pathogenic DNA from different plant species within a minute. During DNA extraction, the polymeric MN patch penetrates into plant leaf tissues and breaks rigid plant cell walls to isolate intracellular DNA. The extracted DNA is polymerase chain reaction (PCR) amplifiable without additional purification. This minimally invasive method has successfully extracted Phytophthora infestans DNA from infected tomato leaves. Moreover, the MN patch could be used to isolate DNA from other plant pathogens directly in the field. Thus, it has great potential to become a rapid, on-site sample preparation technique for plant pathogen detection. © 2020 by John Wiley & Sons, Inc. Basic Protocol: Microneedle patch-based DNA extraction Support Protocol 1: Microneedle patch fabrication Support Protocol 2: Real-time PCR amplification of microneedle patch extracted DNA.

A Rapid, Simple, Laboratory and Field-Adaptable DNA Extraction and Diagnostic Method Suitable for Insect-Transmitted Plant Pathogen and Insect Identification

Watch a presentation about this research by first author Karolina Pusz-Bochenska. Surveillance for insect-transmitted pathogens of plants involves sampling insects in the field, followed by transport of the samples to the laboratory for DNA extraction and molecular analysis. Sample transport and DNA extraction are time consuming and can delay the implementation of measures to mitigate the effects of insect-transmitted plant pathogens. Looking for a fast and reliable method to extract DNA in the field where insects were collected, we used Flinders Technology Associates PlantSaver cards, which are designed for plant DNA extraction. Insect DNA extraction can be achieved in the field, and extracted DNA can be amplified using the field-adaptable method, loop-mediated isothermal amplification (LAMP), in less than 1 h. Additionally, we demonstrate the feasibility and accuracy of the paper extraction method for molecular identification to the species level using mitochondrial cytochrome oxidase 1 amplification and sequencing on 11 genera of insects including beetles, leafhoppers, flies, psyllids, and aphids. The method was suitable for insects collected using three common methods: live-trapped and frozen, stored in ethanol, or trapped on sticky cards. Moreover, by testing leafhoppers collected in 2018 in the field, we demonstrated that the LAMP assay using the chaperonin-60 target detects a higher proportion of samples positive for ‘Candidatus Phytoplasma asteris’ than conventional PCR targeting 16S rRNA. Lastly, the paper extraction method was used to determine the prevalence of leafhoppers carrying the plant pathogenic bacterium ‘Ca. P. asteris’, which causes aster yellows from a laboratory-reared colony using PCR-based tests (conventional PCR, qPCR, and droplet digital PCR) and the non-PCR-based LAMP assay.

Genomic DNA isolation from scrophularieae dried leaves using a simple, high-throughput protocol

This communication described efficient DNA extraction from Scrophularia and Verbascum samples. Modified Murray and Thompson modified Cota-Sànchez method and Bioflux kit methods were applied for the extraction of DNA. Among the different methods, Bioflux kit Plant DNA extraction kit, coupled with some modification was the best for extraction of high molecular weight DNA as long as the extracted DNA is quantified with fluorescence-based methods.

DNA de Solenidium lunatum (Lindl.) Kraenzl (Orchidaceae)

Estudo de caracterização molecular e de diversidade genética com base em marcadores moleculares requer DNA de qualidade, livre de contaminantes como fenóis e polissacarídeos, e também em quantidade suficiente para realização de reações em cadeia da polimerase (PCR). Os protocolos de extração de DNA vegetal são, em sua maioria, baseados no método CTAB (Brometo de Cetiltrimetilamônio), contudo devido às particularidades de cada planta, são necessários ajustes quanto aos reagentes utilizados e à quantidade dos mesmos. Diante do exposto, este estudo teve por objetivo avaliar diferentes concentrações de CTAB e de β-mercaptoetanol no protocolo de extração de DNA de Solenidium lunatum (Lindl.) Kraenzl (Orchidaceae), visando futuros estudos de diversidade genética com utilização de marcadores moleculares. Para o CTAB foram testadas as concentrações 2% e 5%, enquanto que para o β-mercaptoetanol, foram testados 0% e 2%. Para verificar se o material extraído era passível de amplificação, realizam-se testes com três primers ISSR (Inter Simple Sequence Repeats). Os resultados indicam que todos os métodos foram eficientes na extração do DNA em quantidade e qualidade necessárias para realização de PCRs. Todavia, recomenda-se a utilização do protocolo CTAB 2% sem adição de β-mercaptoetanol, uma vez que não foram verificadas diferenças significativas nos resultados de amplificações. A utilização desse protocolo produz material de qualidade, passível de amplificação, com redução de custos e de riscos de intoxicação.

Extraction of Plant DNA by Microneedle Patch for Rapid Detection of Plant Diseases.

In-field molecular diagnosis of plant diseases via nucleic acid amplification is currently limited by cumbersome protocols for extracting and isolating pathogenic DNA from plant tissues. To address this challenge, a rapid plant DNA extraction method was developed using a disposable polymeric microneedle (MN) patch. By applying MN patches on plant leaves, amplification-assay-ready DNA can be extracted within a minute from different plant species. MN-extracted DNA was used for direct polymerase chain reaction amplification of plant plastid DNA without purification. Furthermore, using this patch device, extraction of plant pathogen DNA ( Phytophthora infestans) from both laboratory-inoculated and field-infected leaf samples was performed for detection of late blight disease in tomato. MN extraction achieved 100% detection rate of late blight infections for samples after 3 days of inoculation when compared to the conventional gold standard cetyltrimethylammonium bromide (CTAB)-based DNA extraction method and 100% detection rate for all blind field samples tested. This simple, cell-lysis-free, and purification-free DNA extraction method could be a transformative approach to facilitate rapid sample preparation for molecular diagnosis of various plant diseases directly in the field.

Dryas as a Model for Studying the Root Symbioses of the Rosaceae.

The nitrogen-fixing root nodule symbiosis is restricted to four plant orders: Fabales (legumes), Fagales, Cucurbitales and Rosales (Elaeagnaceae, Rhamnaceae, and Rosaceae). Interestingly all of the Rosaceae genera confirmed to contain nodulating species (i.e., Cercocarpus, Chamaebatia, Dryas, and Purshia) belong to a single subfamily, the Dryadoideae. The Dryas genus is particularly interesting from an evolutionary perspective because it contains closely related nodulating (Dryas drummondii) and non-nodulating species (Dryas octopetala). The close phylogenetic relationship between these two species makes Dryas an ideal model genus to study the genetic basis of nodulation by whole genome comparison and classical genetics. Therefore, we established methods for plant cultivation, transformation and DNA extraction for these species. We optimized seed surface sterilization and germination methods and tested growth protocols ranging from pots and Petri dishes to a hydroponic system. Transgenic hairy roots were obtained by adapting Agrobacterium rhizogenes-based transformation protocols for Dryas species. We compared several DNA extraction protocols for their suitability for subsequent molecular biological analysis. Using CTAB extraction, reproducible PCRs could be performed, but CsCl gradient purification was essential to obtain DNA in sufficient purity for high quality de novo genome sequencing of both Dryas species. Altogether, we established a basic toolkit for the culture, transient transformation and genetic analysis of Dryas sp.

Brief Note Rapid plant DNA and RNA extraction protocol using a bench drill

Plant DNA and RNA extraction methods are well established, with a wide range of protocols, depending on the purposes of each laboratory/research. Nowadays, quick, inexpensive and easy plant DNA and RNA extraction methods are highly sought after. We developed an optimized protocol for plant DNA and RNA extraction that uses an inexpensive bench drill and plastic bags and does not require liquid nitrogen. DNA from leaves and RNA from leaves and roots of banana, pineapple, citrus, papaya, passion fruit and cassava, were extracted using a basic cetyltrimethylammonium bromide method. Both nucleic acids were quantified and evaluated for quality based on agarose gel electrophoresis. The DNA and RNA extractions were successful for all species, and RNA quality in pellets was maintained after storage at room temperature for three weeks. This protocol can reduce costs considerably in laboratories with ongoing routine activities of DNA and RNA extraction for genetic diversity and gene expression analyses, where other conventional methods have not been successful due to explant, condition of samples and quantity and quality of nucleic acids. This is especially relevant for many laboratories in developing countries where the cost and availability of liquid nitrogen may be a constraint.

Comparison of Some Plant DNA Extraction Methods

DNA isolation is a routine procedure when performed in laboratory environment, yet in the field it may still remain problematic. This is especially true of some crop species bred for useful metabolites that may also hinder DNA extraction. Here we compare the efficiency of DNA extraction protocols and commercial DNA isolation kits when used on samples from Helianthus and Allium. Since extraction of DNA is known to be compromised by co-extraction of PCR-inhibiting metabolites, the isolation of DNA was followed by PCR as a testing procedure for the isolation step. The MagnoPrime Fact and MagnoPrime Uni DNA isolation kits were better suited for field work due to faster processing times and smaller required amount of starting material (20 mg fresh/0.5 mg dry). In all cases the subsequent PCR managed to amplify the DNA fragments of interest well enough to be useful in further research.

A novel plant DNA extraction method using filter paper-based 96-well spin plate.

A simple, low cost and safe method using homemade filter paper-based 96-well spin plates and homemade solutions was developed for high throughput plant DNA extraction to use in molecular marker analysis. A low cost and safe method was developed for high throughput extraction of plant DNA for molecular marker analysis. In this method, we describe a simple way to prepare 96-well spin plate using filter paper, a plant material product for DNA binding. Such filter paper-based spin plate can combine with homemade non-toxic buffers for high throughput extraction of plant DNA. We confirmed that filter paper is an efficient solid-phase DNA binding material and comparable to silicon-based glass fiber filters adopted in commercial DNA extraction kits, and that plant DNA extracted by this method can be readily used as template for PCR. The efficacy of this method was also fully demonstrated by molecular marker analysis in segregating populations of tomato. Due to greatly reduced expense compared to commercial kits, this method is of great value for small labs with limited resources.

Evaluation of economical and rapid method of plant DNA extraction for PCR analysis of different crops

In the recent genomic era, polymerase chain reaction (PCR) has become a basic tool in molecular studies and the success of PCR depends upon the template DNA. PCR technique is quite robust and often unnecessary to extract high quality of DNA and hence crude DNA can be used as template for amplification. Therefore, we have evaluated NaOH-Tris DNA extraction method for PCR analysis because this is very simple, time saving and safe without the need to use expensive or rare materials and laboratory apparatus. This method only requires a small amount of leaf tissue, NaOH, Tris, micro tube and plastic pestle. The amplified PCR products showed clear, sharp and uniform bands gave similar results as compared with the modified CTAB method. The DNA obtained is crude contains impurities like protein, RNA but these impurities did not affect PCR amplification. This DNA extraction method is evaluated for brinjal (Solanummelongena L.), chilli (Capsicum annuum L.), rice (Oryza sativa L.) and tomato (Solanumlycopersicum L.) crop. Many other crop plants could also be amplified using the same DNA extraction method for molecular analysis of large samples. Thus, the use of NaOH-Tris method will allow researchers to obtain DNA from plant quickly for use in molecular studies.

Species diversity and utilization of bamboo to support life’s the community of Karangwangi Village, Cidaun Sub-District of Cianjur, Indonesia

Abstract. Hailu HW, Sajidan, Pangastuti A, GreinerR. 2017. Isolation, characterization and 18S rDNA sequence analysis of phytase producing fungi from Indonesia, Indonesia. Biodiversitas 18: 10-14. Phytase breaks down the phytate portion of grains and oil seeds; thereby, releasing phosphorus and minerals for animals. The objectives of this research were to screen phytase-producing novel species of fungi; to conduct cultural and phylogenetic characterization; to perform 18S rDNA sequencing and BLAST analysis. Samples of fungi were collected from different sources, cultured on potato dextrose agar and potato dextrose broth. Phytase assay was conducted based on Vanadate-molybdate method. Three isolates with highest enzyme activity were selected for pH and temperature optimization. DNA was extracted by modifying plant DNA extraction and yeast genomic DNA extraction kits. The 18S rDNA gene was amplified and sequenced. The result indicated that optimum temperatures ranged from 60-75oC and the optimum pH for isolates from papaya (Angr), palm bark (Abark) and sugarcane soil field (Asoil) were 4.5, 3.0 and 4.5, respectively. Based on 18S rDNA sequence analysis the phytase producing fungal isolates Angr, Abark and Asoil were identical to Aspergillus niger, Beauveria felina and Nigrosabulum globosum, respectively.Keywords: 18S rDNA, BLAST, fungi, phytase, phylogeny

GENETIC STABILITY ANALYSIS OF RB GENE IN GENETICALLY MODIFIED POTATO LINES TOLERANT TO Phytophthora infestans

Development of potato cultivars with high levels of broad spectrum resistance is a key long-term management strategy against late blight disease caused by Phytophthora infestans. Six progeny lines of hybridization between transgenic potato Katahdin SP951 with non-transgenic Granola and Atlantic were selected based on agronomical characteristics and resistance to late blight disease. The study aimed to analyze the number of insertions and stability of inserted RB gene in the transgenic potato lines. The research was carried out through plant DNA extraction, southern blot analysis and polymerase chain reaction (PCR). Southern blot analysis was used to detect the number of inserts integrated into potato genome, while PCR analysis was used to detect stability of RB gene from generation to generation. The results showed that the progenies obtained from hybridization between Atlantic and transgenic Katahdin SP951 (lines No. 20 and 27) and between Granola and transgenic Katahdin SP951 (line No. 69) contained one copy number of RB gene, according to the probing of nptII. The result is similar to that of inserted RB gene found in the parental transgenic Katahdin SP951. The presence of RB gene in four different generations (G0, G1, G2 and G3) showed stable integration of the gene into the plant genome. The single copy number of RB gene will repress the occurrence of silencing gene expression. The stability analysis of RB gene can determine that the gene is still present in plant genome after several generations.

GENETIC STABILITY ANALYSIS OF RB GENE IN GENETICALLY MODIFIED POTATO LINES TOLERANT TO Phytophthora infestans

Development of potato cultivars with high levels of broad spectrum resistance is a key long-term management strategy against late blight disease caused by Phytophthora infestans. Six progeny lines of hybridization between transgenic potato Katahdin SP951 with non-transgenic Granola and Atlantic were selected based on agronomical characteristics and resistance to late blight disease. The study aimed to analyze the number of insertions and stability of inserted RB gene in the transgenic potato lines. The research was carried out through plant DNA extraction, southern blot analysis and polymerase chain reaction (PCR). Southern blot analysis was used to detect the number of inserts integrated into potato genome, while PCR analysis was used to detect stability of RB gene from generation to generation. The results showed that the progenies obtained from hybridization between Atlantic and transgenic Katahdin SP951 (lines No. 20 and 27) and between Granola and transgenic Katahdin SP951 (line No. 69) contained one copy number of RB gene, according to the probing of nptII. The result is similar to that of inserted RB gene found in the parental transgenic Katahdin SP951. The presence of RB gene in four different generations (G0, G1, G2 and G3) showed stable integration of the gene into the plant genome. The single copy number of RB gene will repress the occurrence of silencing gene expression. The stability analysis of RB gene can determine that the gene is still present in plant genome after several generations.

Grapevine yellows: Comparison of different procedures for DNA extraction and amplification with PCR for routine diagnosis of phytoplasmas in grapevine

In order to devise a procedure to be used as reference for detection of grapevine phytoplasmas and monitoring of Flavescence doree, 12 combinations comprising three methods of plant DNA extraction and 4 procedures for amplification in polymerase chain reaction of phytoplasma DNA were examined in parallel using the same plant tissues infected with phytoplasmas. In a first series tissues of periwinkles ( Catharanthus roseus ) infected with phytoplasma isolates of the Elm yellows group (16SrV) and maintained in the greenhouse, were used. In a second series tissues of grapevines ( Vitis vinifera ) naturally infected with Flavescence doree or Palatinate grapevine yellows phytoplasma were used. The DNA preparations obtained with each of the three extraction procedures were used undiluted or serially diluted, as target DNA in the 4 nested-polymerase chain reactions. The results showed differences in the efficiency among different methods of extraction as well as in the sensitivity among the DNA amplification procedures, which improved when DNA extracted from field grapevines was diluted. After additional comparative validation on numerous field-collected samples of GY-affected grapevines, the quickest extraction procedure was selected for use in routine diagnosis, with nested-PCR amplification either of ribosomal DNA or of the FD9 DNA fragment specific for Flavescence doree and other 16SrV group phytoplasmas.

Simple DNA extraction method for SSR-PCR analysis from different tissues ofTapiscia sinensis, an endangered plant species

A simple and rapid method to process different tissues of Tapiscia sinensis for effective plant DNA extraction were established in the study. DNA quality and yield obtained from bark, leaves and seeds were evaluated by Eppendorf BioPhotometer and SSR-PCR analysis. The results indicated that extracted genomic DNA based on the established method was sufficient for SSR-PCR profiling of different tree tissues. Hence, the sample treatment and extraction method can be used for SSR-PCR applications in tree genetic and molecular analysis research.

CONTRIBUTION OF WESTERN AND EASTERN SPECIES TO THE IRANIAN PEAR GERMPLASM REVEALED BY THE CHARACTERIZATION OF S-GENOTYPES

CONTRIBUTION OF WESTERN AND EASTERN SPECIES TO THE IRANIAN PEAR GERMPLASM REVEALED BY THE CHARACTERIZATION OF S-GENOTYPES